Published in J Clin Psychopharmacol on August 01, 2004
Obesity in general elective surgery. Lancet (2003) 7.22
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. Nat Genet (2009) 6.21
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies. Brain (2009) 3.96
Retracted Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies. Nat Genet (2003) 2.70
TDP-43 is recruited to stress granules in conditions of oxidative insult. J Neurochem (2009) 2.57
Use of severely steatotic grafts in liver transplantation: a matched case-control study. Ann Surg (2007) 2.53
Confirmation of association of the GABRA2 gene with alcohol dependence by subtype-specific analysis. Psychiatr Genet (2006) 2.50
EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)--revised report of an EFNS task force. Eur J Neurol (2011) 2.27
Heralded entanglement between widely separated atoms. Science (2012) 2.16
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. Hum Mol Genet (2009) 2.12
Quinine for muscle cramps. Cochrane Database Syst Rev (2010) 1.80
A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions. Arch Neurol (2002) 1.77
Association of a functional BDNF polymorphism and anxiety-related personality traits. Psychopharmacology (Berl) (2005) 1.77
Superiority of small islets in human islet transplantation. Diabetes (2007) 1.76
The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder. Eur J Hum Genet (2012) 1.71
Is the acetabular cup orientation after total hip arthroplasty on a two dimension or three dimension model accurate? Int Orthop (2014) 1.62
Expression pattern and functional characteristics of two novel splice variants of the two-pore-domain potassium channel TREK-2. J Physiol (2002) 1.56
Laparoscopic versus open splenectomy for nontraumatic diseases. World J Surg (2008) 1.55
Psychosocial impact of living-related kidney transplantation on donors and partners. Pediatr Nephrol (2004) 1.50
Finding the right position: a three-year, single-center experience with the "self-locating" catheter. Perit Dial Int (2010) 1.49
LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures. Ann Neurol (2002) 1.48
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. Hum Mol Genet (2012) 1.48
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. Ann Neurol (2011) 1.45
Human aging magnifies genetic effects on executive functioning and working memory. Front Hum Neurosci (2008) 1.41
New device for the introduction of a circular stapler in laparoscopic gastric bypass surgery. Obes Surg (2006) 1.40
Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy. Ann Neurol (2004) 1.40
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect. Am J Hum Genet (2011) 1.39
Apoptosis in hypoxic human pancreatic islets correlates with HIF-1alpha expression. FASEB J (2002) 1.36
Robotic-assisted versus laparoscopic cholecystectomy: outcome and cost analyses of a case-matched control study. Ann Surg (2008) 1.35
Observation of entanglement of a single photon with a trapped atom. Phys Rev Lett (2006) 1.28
Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2. Epilepsy Res (2003) 1.26
CLCN2 variants in idiopathic generalized epilepsy. Nat Genet (2009) 1.26
Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients. Hum Mol Genet (2011) 1.24
DEPDC5 mutations in genetic focal epilepsies of childhood. Ann Neurol (2014) 1.21
Two corticosteroid-free regimens-tacrolimus monotherapy after basiliximab administration and tacrolimus/mycophenolate mofetil-in comparison with a standard triple regimen in renal transplantation: results of the Atlas study. Transplantation (2005) 1.17
Candidate gene analysis identifies a polymorphism in HLA-DQB1 associated with clozapine-induced agranulocytosis. J Clin Psychiatry (2010) 1.16
Catechol-O-methyltransferase val158met genotype influences neural processing of reward anticipation. Neuroimage (2008) 1.12
Gender differences in the performance of a computerized version of the alcohol use disorders identification test in subcritically injured patients who are admitted to the emergency department. Alcohol Clin Exp Res (2004) 1.12
The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect. Neurobiol Dis (2011) 1.12
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy. Ann Neurol (2014) 1.11
Central necrosis in isolated hypoxic human pancreatic islets: evidence for postisolation ischemia. Cell Transplant (2005) 1.11
Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24. Epilepsia (2002) 1.09
Association of the met66 allele of brain-derived neurotrophic factor (BDNF) with smoking. Psychopharmacology (Berl) (2006) 1.09
Comparison of ligand- and structure-based virtual screening on the DUD data set. J Chem Inf Model (2009) 1.08
Exploration of the genetic architecture of idiopathic generalized epilepsies. Epilepsia (2006) 1.07
Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore. Mol Pharmacol (2008) 1.07
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy. Epilepsia (2013) 1.07
Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy. Am J Med Genet B Neuropsychiatr Genet (2007) 1.06
Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and mice. Am J Hum Genet (2007) 1.06
The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily of leucine-rich repeat proteins. FEBS Lett (2002) 1.06
Motor unit number index (MUNIX): a novel neurophysiological technique to follow disease progression in amyotrophic lateral sclerosis. Muscle Nerve (2010) 1.05
Gender-dependent association of the functional catechol-O-methyltransferase Val158Met genotype with sensation seeking personality trait. Neuropsychopharmacology (2007) 1.05
Motor Unit Number Index (MUNIX): a novel neurophysiological marker for neuromuscular disorders; test-retest reliability in healthy volunteers. Clin Neurophysiol (2011) 1.05
Neurophysiological measures in amyotrophic lateral sclerosis: markers of progression in clinical trials. Amyotroph Lateral Scler Other Motor Neuron Disord (2005) 1.05
KIBRA and CLSTN2 polymorphisms exert interactive effects on human episodic memory. Neuropsychologia (2009) 1.04
Uptake, efficacy, and systemic distribution of naked, inhaled short interfering RNA (siRNA) and locked nucleic acid (LNA) antisense. Mol Ther (2011) 1.03
Event-related potentials associated with Attention Network Test. Int J Psychophysiol (2010) 1.03
Association of the G1947A COMT (Val(108/158)Met) gene polymorphism with prefrontal P300 during information processing. Biol Psychiatry (2003) 1.02
Functionality of the GAL4/UAS system in Tribolium requires the use of endogenous core promoters. BMC Dev Biol (2010) 1.00
Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. Epilepsia (2013) 0.99
Laparoscopic pouch resizing and redo of gastro-jejunal anastomosis for pouch dilatation following gastric bypass. Obes Surg (2005) 0.98
HIV-specific cellular immune response is inversely correlated with disease progression as defined by decline of CD4+ T cells in relation to HIV RNA load. J Infect Dis (2004) 0.98
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy. Epilepsia (2007) 0.98
Variations in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) are associated with bipolar i disorder. Neuropsychopharmacology (2006) 0.97
Association of attentional network function with exon 5 variations of the CHRNA4 gene. Hum Mol Genet (2007) 0.97
Pregabalin versus pramipexole for restless legs syndrome. N Engl J Med (2014) 0.96
A novel class of immune-stimulatory CpG oligodeoxynucleotides unifies high potency in type I interferon induction with preferred structural properties. Oligonucleotides (2010) 0.96
RBFOX1 and RBFOX3 mutations in rolandic epilepsy. PLoS One (2013) 0.95
Clozapine-induced agranulocytosis and its genetic determinants. Pharmacogenomics (2008) 0.95
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. Epilepsia (2012) 0.94
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits. Neurobiol Dis (2005) 0.94
Motor Unit Number Index (MUNIX): reference values of five different muscles in healthy subjects from a multi-centre study. Clin Neurophysiol (2011) 0.93
Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests. Hum Hered (2010) 0.93
Selective anterior cingulate cortex deficit during conflict solution in schizophrenia: an event-related potential study. J Psychiatr Res (2006) 0.93
A novel SOD1 splice site mutation associated with familial ALS revealed by SOD activity analysis. Hum Mol Genet (2010) 0.92
No difference in clinical outcome, bone density and polyethylene wear 5-7 years after standard navigated vs. conventional cementfree total hip arthroplasty. Arch Orthop Trauma Surg (2015) 0.92
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta. BMC Med Genet (2011) 0.92
HIV-1 does not provoke alteration of cytokine gene expression in lymphoid tissue after acute infection ex vivo. J Immunol (2004) 0.92
Combined nephrectomy and pre-emptive renal transplantation in a tuberous sclerosis patient with angiomyolipoma, renal carcinoma and life-threatening abdominal haemorrhages. Nephrol Dial Transplant (2007) 0.92
Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4. Headache (2006) 0.92
Hepatocellular carcinoma and liver transplantation: entering the area after the Milan and University of California at San Francisco criteria? Liver Transpl (2008) 0.92
Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy. Ann Neurol (2005) 0.91
A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy. Epilepsy Res (2005) 0.91
Physical and psychosocial outcome in morbidly obese patients with and without bariatric surgery: a 4 1/2-year follow-up. Obes Surg (2006) 0.91
Probing the Drosophila retinal determination gene network in Tribolium (II): The Pax6 genes eyeless and twin of eyeless. Dev Biol (2009) 0.91
Ebbinghaus revisited: influences of the BDNF Val66Met polymorphism on backward serial recall are modulated by human aging. J Cogn Neurosci (2010) 0.90
Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome. Epilepsia (2011) 0.90
Executive attention in schizophrenic males and the impact of COMT Val108/158Met genotype on performance on the attention network test. Schizophr Bull (2008) 0.90
Association of CYP2D6 genotypes and personality traits in healthy individuals. J Clin Psychopharmacol (2006) 0.90
Association of BRD2 polymorphisms with photoparoxysmal response. Neurosci Lett (2006) 0.90
The Edinburgh Cognitive and Behavioural Amyotrophic Lateral Sclerosis Screen: a cross-sectional comparison of established screening tools in a German-Swiss population. Amyotroph Lateral Scler Frontotemporal Degener (2014) 0.89
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement. J Neurol (2013) 0.89
Treatment for cramps in amyotrophic lateral sclerosis/motor neuron disease. Cochrane Database Syst Rev (2012) 0.89
Attitudes towards hastened death in ALS: a prospective study of patients and family caregivers. Amyotroph Lateral Scler Frontotemporal Degener (2013) 0.88
Met carriers of BDNF Val66Met genotype show increased N-acetylaspartate concentration in the anterior cingulate cortex. Neuroimage (2009) 0.88
Association of HTR2C, but not LEP or INSIG2, genes with antipsychotic-induced weight gain in a German sample. Pharmacogenomics (2010) 0.88